Correlation of two different devices for the evaluation of primary implant stability depending on dental implant length and bone density: An in vitro study.

Non-invasive objective implant stability measurements are needed to determine the appropriate timing of prosthetic fitting after implant placement. We compared the early implant stability results obtained using resonance frequency analysis (RFA) and damping capacity analysis (DCA) depending on the implant length and bone density. Total 60, 4.0 mm diameter implants of various lengths (7.3 mm, 10 mm, and 13 mm) were used. In Group I, low-density bone was described using 15 PCF (0.24 g/cm3) polyurethane bone blocks, and in Group II, 30 PCF (0.48 g/cm3) polyurethane bone blocks were used to describe medium density bone. RFA was performed using an Osstell® Beacon+; DCA was performed using Anycheck®. Measurements were repeated five times for each implant. Statistical significance was set at P <0.05. In Group I, bone density and primary implant stability were positively correlated, while implant length and primary implant stability were positively correlated. In Group II, the implant stability quotient (ISQ) and implant stability test (IST) values in did not change significantly above a certain length. Primary implant stability was positively correlated with bone density and improved with increasing implant length at low bone densities. Compared with the Osstell® Beacon+, the simplicity of Anycheck® was easy to use and accessible.

A One-Year Randomized Controlled Clinical Trial of Three Types of Narrow-Diameter Implants for Fixed Partial Implant-Supported Prosthesis in the Mandibular Incisor Area.

Narrow-diameter implants (NDI) serve as a solution for treating limited bone volume in the anterior mandible. This study aimed to evaluate the one-year clinical outcomes of various NDIs in the mandibular incisor area after immediate loading in partially edentulous patients. This single-center, prospective, single-blinded, randomized controlled trial study included 21 patients, with 7 patients in each of the following groups: control (BLT NC SLActive®; Straumann), experimental group 1 (CMI IS-III Active® S-Narrow; Neobiotech), and experimental group 2 (CMI IS-III Active® Narrow; Neobiotech). Using full digital flow, two fixtures were placed in each patient and immediately provisionalized on the day of surgery. Evaluations encompassed periapical radiographs, implant stability quotient (ISQ), implant stability test (IST) readings, per-implant soft tissue health, patient satisfaction surveys, and esthetic score assessments. Definitive prostheses were delivered twelve weeks post-surgery (CRiS, number: KCT0007300). Following exclusions due to low stability values (n = 2), fixture failure (n = 5), and voluntary withdrawal (n = 1), the implant success rate for patients completing all clinical protocols stood at 100%. The resulting patient failure rates in the control, experimental group 1, and experimental group 2 were 50.0%, 42.9%, and 14.3%, respectively. There were no significant differences between the groups in terms of marginal bone loss, soft tissue health, patient satisfaction, and esthetic scores. Narrow implants showed superior clinical outcomes, followed by S-Narrow and Straumann implants. Calculated one-year survival rates at the implant level were 66.7% for the control group, 85.7% for experimental group 1, and 100% for experimental group 2. All three types of NDIs showed acceptable clinical and radiographic results during the year-long observation period.

Comparison of Implant Surgery Methods of Cortical Tapping and Cortical Widening in Bone of Various Density: A Three-Dimensional Finite Element Study.

PURPOSE: The primary stability of a dental implant is critical for successful osseointegration during immediate loading. The cortical bone should be prepared to achieve enough primary stability, but not overcompressed. In this study, we investigated the stress and strain distribution in the bone around the implant induced by the occlusal force applied during immediate loading at various bone densities by the FEA method to compare cortical tapping and widening surgical techniques. MATERIALS AND METHODS: A three-dimensional geometrical model of a dental implant and bone system was created. Five types of bone density combination (D111, D144, D414, D441 and D444) were designed. Two surgical methods-cortical tapping and cortical widening-were simulated in the model of the implant and bone. An axial load of 100 N and an oblique load of 30 N were applied to the crown. The maximal principal stress and strain were measured for comparative analysis of the two surgical methods. RESULTS: Cortical tapping showed lower maximal stress of bone and maximal strain of bone than cortical widening when dense bone was located around the platform, regardless of the direction of the applied load. CONCLUSIONS: Within the limitations of this FEA study, it can be concluded that cortical tapping is biomechanically more advantageous to the implants under occlusal force during immediate loading, especially when the bone density around the platform is high.

Effect of custom abutment data superimposition on the accuracy of implant abutment level scanning: An in vitro study.

STATEMENT OF PROBLEM: When scanning implant abutments, an incomplete scan is often obtained because of a subgingival location or restricted accessibility. Whether these problems can be overcome with a novel scanning technique with digital superimposition of the custom abutment is unclear. PURPOSE: The purpose of this in vitro study was to evaluate the effect of the process of superimposing the custom abutment library data onto the scanned abutment data on the accuracy of the digital scan with an intraoral scanner. MATERIAL AND METHODS: A model with a single implant was prepared. The custom abutment of the corresponding implant was produced and was scanned with a laboratory scanner to produce the custom abutment library data. The custom abutment was connected to the implant, and the model was scanned with a laboratory scanner for the reference data. The custom abutment and adjacent teeth were scanned 10 times with an intraoral scanner. Thus, 10 files were saved as the first test group (IOS). After transferring 10 files of the group IOS to a computer-aided design (CAD) software program (exocad DentalCAD), the custom abutment library data were superimposed on the corresponding abutments, and the results were saved as the second test group (S-Exo). For the third test group (S-Den), the same superimposing process was performed as for the group S-Exo but by using another CAD software program (Dental System). The accuracy of the files of the 3 test groups was evaluated by comparing them with the reference file by using a 3D inspection software program. Statistical analysis was performed with 1-way repeated measures ANOVA (α=.05). RESULTS: The RMS of the IOS group decreased significantly from 42.1 ±1.1 µm to 36.37 ±0.74 µm for the S-Exo group and 36.89 ±0.69 µm for the S-Den group after superimposition (P<.05). InTOL increased significantly from 88.17 ±0.75% to 91.57 ±0.56% in the S-Exo group and 91.31 ±0.56% in the S-Den group (P<.05). For the mean 3D discrepancy of all 66 points along the margin and 16 points of interest, the IOS group showed significantly higher discrepancy than the superimposed groups (P<.05), implying that the accuracy of scanned data with the intraoral scanner increased after superimposition with the abutment library data. No significant difference was found according to the type of software program (P>.05). CONCLUSIONS: The process of superimposing the titanium custom abutment with the prescanned custom abutment library data improved the accuracy of a digital scan made with an intraoral scanner.

Effect of scanning-aid agents on the scanning accuracy in specially designed metallic models: A laboratory study.

The advent of intraoral scanning methods has caused a paradigm shift in dentistry. However, despite their many advantages, intraoral scanners cannot accurately recognize the metallic surfaces of prothesis. Therefore, this experiment was designed to verify the effect of scanning-aid agents on the scanning accuracy using metallic reference models. Three different types of metallic reference models (inlay, onlay, and bridge) were specially designed and produced using a milling machine to simulate intraoral dental restorations. Three experimental groups (application of ScanCure, IP Scan Spray, and VITA Powder Scan Spray) were set up and scanned images (each n = 5) were acquired using the I500® intraoral scanner. The reference datasets were established by a 3D design that reflected the deviations between the measured distances and previously planned distances on the reference models. All acquired experimental datasets were digitally superimposed and compared with the reference datasets. Intragroup comparisons (precision, n = 10) were also performed. The root mean square (RMS) values of trueness in the ScanCure and IP groups were significantly more accurate than those of the VITA group in the inlay and onlay reference models (p < 0.05). Notably, in the bridge reference model, the liquid-type ScanCure group showed the highest accuracy of trueness, with statistical significance (p < 0.05). However, the RMS values of precision were not significantly different among the groups. These findings suggest that liquid-type scanning agents can be effectively used to obtain more accurate scan images of intraoral metallic dental restorations.

Influence of Scanning-Aid Materials on the Accuracy and Time Efficiency of Intraoral Scanners for Full-Arch Digital Scanning: An In Vitro Study.

This study was performed to verify the influence of scanning-aid materials on the accuracy and time efficiency of full-arch scanning with intraoral scanners. The full-arch reference model was constructed by a 3D printer and scanned with a model scanner to obtain the reference dataset. Four experimental groups (application of ScanCure (SC-80, ODS Co, Incheon, Korea), IP Scan Spray (IP-Division, Haimhausen, Germany) and Vita Powder Scan Spray (Vita Zahnfabrik, Stuttgart, Germany), and no treatment) were designed, and the scans were executed (trueness, n = 5) using two intraoral scanners: I500 (Medit Co., Seoul, Korea) and TRIOS (3shape, Copenhagen, Denmark). All acquired scan data were compared with the reference datasets using the 3D superimposition method and 2D linear measurements. In the 3D analysis, intragroup data were compared with each other (precision, n = 10). Time efficiency was also verified by comparing the scan times of the four experimental groups. In the 3D analysis, the root mean square (RMS) value of the precision of the scanned image was statistically significantly more accurate in the scanning-aid agent-treated groups than in the no-treatment group (p < 0.05). However, the RMS values of trueness and the types of scanning-aid materials were not significantly different. In the 2D measurements, the increased scan distance generated a greater distance deviation. The working time was significantly shorter in the scanning-aid agent groups than in the no-treatment group, with statistical significance (p < 0.05). Therefore, in clinical situations, the application of scanning-aid materials is recommended to reduce scanning time and more efficiently obtain the full-arch scanned image.

Restoration of a partially edentulous patient with an implant-supported removable partial denture: a case report.

The aim of this report is to present and discuss the clinical procedure of an implant-supported removable partial denture for a partially edentulous patient who exhibited a severely resorbed ridge and a collapsed vertical stop. The 67-year-old partially edentulous patient presented with a lack of vertical stop and an advanced transverse arch discrepancy. For the maxilla, an implant-supported removable partial denture was fabricated on bilateral distal implant abutments. The mandibular arch was restored with an implant-supported fixed partial denture, since it was expected to function more properly than a removable partial denture. This clinical report demonstrates a successful treatment approach to restore oral function and appearance for the patient.